ClearanceBrief
Recall Z-2017-2023 ยท EOQ Bronchoscope (Flexible Or Rigid)

Olympus Corporation of the Americas

Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-H190, BF-Q190, BF-XT190, BF-1TH190

DateJul 17, 2023 (initiated Jun 8, 2023)
StatusOpen, Classified
ReasonThere have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Root causeUnder Investigation by firm
ActionAn "URGENT MEDICAL DEVICE CORRECTIVE ACTION" notification letter dated 6/8/23 was sent to customers. Actions to be taken by the company: The labelling will be updated to include specificity about laser compatibility, improved instructions regarding patient preparation, and warnings about patient injury and death resulting from incompatible laser use. Actions to be taken by the end user: 1. Inspect your inventory for the referenced devices and identify any device with the model names. Please check all areas of the hospital to determine if any of these devices remain in inventory. 2. Carefully
Quantity9,684 units
DistributionUS Nationwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K121959EVIS EXERA III VIDEO SYSTEM
Olympus Medical Systems Corp., Jan 10, 2013
K183419EVIS EXERA III Bronchovideoscope Olympus BF-XT190
Olympus Medical Systems Corp., Sep 5, 2019